5th HQ
Manufacturing Manager
Skills
1 year ago
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Important information
Contract type:
Permanent
Salary:
$62,400 / year
Location:
Miramar, FL, USA
Work mode:
Onsite
Published on:
15 October 2026
What they need
We are seeking an experienced Manufacturing Manager to lead and oversee day-to-day operations within our nutraceutical/pharmaceutical production facility. The ideal candidate will bring proven leadership in cGMP-compliant environments and possess a strong background in managing production teams, ensuring regulatory compliance, and driving continuous improvement in quality, efficiency, and safety.
Location: Miramar, FL
Compensation: $30 per hour
Schedule:
- Standard Office Hours: 8:30 AM – 5:00 PM
- Flex Shift (as needed): 10:00 AM – 7:00 PM
Preferred Background:
- Prior experience in nutraceutical or pharmaceutical manufacturing is highly preferred.
- Strong understanding of OSHA, FDA, and cGMP regulations.
- Familiarity with world-class manufacturing methods and statistical process control.
Minimum Qualifications:
- Bachelor’s Degree (B.A. or B.S.) required.
- 4–5 years of manufacturing supervisory experience in a cGMP-regulated facility.
- Strong leadership and team-building skills.
- Excellent verbal and written communication skills.
- Proven ability to analyze production performance and implement improvements.
- Working knowledge of manufacturing documentation, SOPs, and quality control practices.
Key Responsibilities:
- Lead and manage the manufacturing department, ensuring smooth daily operations and alignment with company goals.
- Report directly to the COO while collaborating cross-functionally with QC, Sales, Operations, CEO, and CFO.
- Establish and enforce production procedures to maintain high-quality standards, safety, and operational efficiency.
- Ensure compliance with cGMP, SOPs, and company quality systems.
- Oversee production scheduling, staffing, and shift planning—including managing overtime and additional shifts as necessary.
- Monitor production runs to ensure they stay on schedule and troubleshoot any delays or issues.
- Continuously evaluate and improve efficiency, machine utilization, and resource allocation.
- Oversee batch record documentation, ensuring accuracy, completeness, and compliance with regulations.
- Analyze finished goods (capsules and tablets) to ensure they meet specifications for potency, weight, and quality.
- Provide regular training to team members on GMP practices, SOP compliance, and safety procedures.
- Promote a clean, organized, and accident-free work environment by enforcing all safety protocols.
- Identify areas for cost savings and implement strategies for lean manufacturing and continuous improvement.
Preferred Skills & Traits:
- Bilingual (English/Spanish) is a plus.
- Proficient in Microsoft Office and experience with ERP systems.
- Knowledge of Lean Manufacturing, Six Sigma, or similar process improvement methodologies is beneficial.
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